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Journal Abstract Search

176 related items for PubMed ID: 8096494

  • 1. Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.
    Hydén-Granskog C, Salonen R, von Koskull H.
    Hum Genet; 1993 Mar; 91(2):185-9. PubMed ID: 8096494
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  • 3. A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28.
    Curtis AR, Lindsay S, Boye E, Clarke AJ, Landy SJ, Bhattacharya SS.
    Eur J Hum Genet; 1994 Mar; 2(1):51-8. PubMed ID: 7913867
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  • 5. X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation.
    Woffendin H, Jakins T, Jouet M, Stewart H, Landy S, Haan E, Harris A, Donnai D, Read A, Kenwrick S.
    Clin Genet; 1999 Jan; 55(1):55-60. PubMed ID: 10066033
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  • 9. Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.
    Sefiani A, Sinnett D, Abel L, Szpiro-Tapia S, Heuertz S, Craig I, Fraser N, Kruse TA, Frydman M, Peter MO.
    Hum Genet; 1988 Nov; 80(3):282-6. PubMed ID: 3192215
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  • 10. The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28.
    Smahi A, Hyden-Granskog C, Peterlin B, Vabres P, Heuertz S, Fulchignoni-Lataud MC, Dahl N, Labrune P, Le Marec B, Piussan C.
    Hum Mol Genet; 1994 Feb; 3(2):273-8. PubMed ID: 8004094
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  • 13. Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation.
    Cannizzaro LA, Hecht F.
    Clin Genet; 1987 Jul; 32(1):66-9. PubMed ID: 3621656
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  • 16. Gonadal mosaicism for incontinentia pigmenti in a healthy male.
    Kirchman TT, Levy ML, Lewis RA, Kanzler MH, Nelson DL, Scheuerle AE.
    J Med Genet; 1995 Nov; 32(11):887-90. PubMed ID: 8592334
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